Evidence map›Paper›PMID 32117426›Full record

ArticleFrontiers in genetics2019

Evaluation of Pathway Activation for a Single Sample Toward Inflammatory Bowel Disease Classification.

Xingyi Li, Min Li, Ruiqing Zheng, Xiang Chen, Ju Xiang, Fang-Xiang Wu, Jianxin Wang

Abstract read
In one paragraph

Article in Frontiers in genetics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

7 authors.

Xingyi LiSchool of Computer Science and Engineering, Central South University, Changsha, China.
Min LiSchool of Computer Science and Engineering, Central South University, Changsha, China.
Ruiqing ZhengSchool of Computer Science and Engineering, Central South University, Changsha, China.
Xiang ChenSchool of Computer Science and Engineering, Central South University, Changsha, China.
Ju XiangSchool of Computer Science and Engineering, Central South University, Changsha, China.
Fang-Xiang WuDepartment of Mechanical Engineering and Division of Biomedical Engineering, University of Saskatchewan, Saskatoon, SK, Canada.
Jianxin WangSchool of Computer Science and Engineering, Central South University, Changsha, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Since similar complex diseases are much alike in clinical symptoms, patients are easily misdiagnosed and mistreated. It is crucial to accurately predict the disease status and identify markers with high sensitivity and specificity for classifying similar complex diseases. Many approaches incorporating network information have been put forward to predict outcomes, but they are not robust because of their low reproducibility. Several pathway-based methods are robust and functionally interpretable. However, few methods characterize the disease-specific states of single samples from the perspective of pathways. In this study, we propose a novel framework, Pathway Activation for Single Sample (PASS), which utilizes the pathway information in a single sample way to better recognize the differences between two similar complex diseases. PASS can mainly be divided into two parts: for each pathway, the extent of perturbation of edges and the statistic difference of genes caused by a single disease sample are quantified; then, a novel method, named as an AUCpath, is applied to evaluate the pathway activation for single samples from the perspective of genes and their interactions. We have applied PASS to two main types of inflammatory bowel disease (IBD) and widely verified the characteristics of PASS. For a new patient, PASS features can be used as the indicators or potential pathway biomarkers to precisely diagnose complex diseases, discover significant features with interpretability and explore changes in the biological mechanisms of diseases.

Indexed as

inflammatory bowel diseasepathway activationpathway biomarkerssimilar complex diseasessingle sample

Identifiers

PMID32117426
PMCPMC7013001

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